Global Site Management Lead, Clinical Research

AbbVie; Madrid; Presencial; EUR 90.000 - 120.000; Jornada completa

Descripción de la vacante

AbbVie seeks an experienced Senior/Global Site Management leader to direct CSM integrity, quality, and timeliness across assigned studies. You will shape the study-level CSM strategy and collaborate with global and country teams to drive site activation, engagement, and close-out, ensuring regulatory readiness.

You will manage resources, monitor risk, and maintain TMF artifacts, with a focus on cross-functional leadership in a matrix environment and fluency in English to communicate with global

Formación

• Bachelor’s Degree in a (para)medical or scientific field.
• Minimum 5 years of industry clinical research experience and preferred 2 years in monitoring or project management on a global study.
• Experience across multiple therapeutic areas and strong leadership abilities.
• Excellent written and verbal English communication skills.
• Ability to influence in a matrix environment and manage study timelines.

Responsabilidades

• Lead study-level CSM strategy and timelines to ensure feasibility and on-time delivery.
• Communicate CSM resource needs with Country Leaders aligned to milestones.
• Accountable for study-level site monitoring strategy and Site Engagement Strategy.
• Drive site activation, engagement, protocol adherence and close-out activities.
• Oversee monitoring activities with other SMLs; track quality and milestones.
• Contribute to Risk Assessment and Mitigation Plan (RAMP) and TMF completeness for CSM artifacts.

Conocimientos

Project management

Leadership

Communication

Risk assessment

Stakeholder management

Fluent English

Matrix environment

Educación

Bachelor's degree

Herramientas

Microsoft Word

Microsoft PowerPoint

Microsoft Excel

Microsoft OneNote

Descripción del empleo

AbbVie seeks an experienced Senior/Global Site Management leader to direct CSM integrity, quality, and timeliness across assigned studies. You will shape the study-level CSM strategy and collaborate with global and country teams to drive site activation, engagement, and close-out, ensuring regulatory readiness.

You will manage resources, monitor risk, and maintain TMF artifacts, with a focus on cross-functional leadership in a matrix environment and fluency in English to communicate with global